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publicationDate 1990-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4904797-A
titleOfInvention Process of preparing cycloalkano(1,2-B)indole-sulphonamides
abstract Cycloalkano[1,2-b]indole-sulphonamides of the formula ##STR1## where appropriate in an isomeric form, and their salts are disclosed. These compounds are useful to inhibit platelet aggregation and to antagonize thromboxane A 2 .
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID521471
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226446335
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14130453
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129936527
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127923761
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226819719
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129617515
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID737070
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14130451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226411656
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54284723
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID798
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8892
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID223758797
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399157
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID30555
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8255
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14130464
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226414568
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136268088
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14130462
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7516
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7618
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14130472
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129287207
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135894632
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129273733
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6364

Total number of triples: 649.